Cleared Traditional

K923173 - OBALON COVER

K923173 is an FDA 510(k) clearance for OBALON COVER, manufactured by Turnsoft, Inc.. The device is a Class 1 General Hospital device with product code FMW cleared through the Traditional 510(k) pathway after a 129-day FDA review.

K923173 · Turnsoft, Inc. · General Hospital
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Nov 1992
Decision
129d
Days
Class 1
Risk

K923173 is an FDA 510(k) clearance for the OBALON COVER. Classified as Cover, Mattress (medical Purposes) (product code FMW), Class I - General Controls.

Submitted by Turnsoft, Inc. (Huntersville, US). The FDA issued a Cleared decision on November 6, 1992 after a review of 129 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6190 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Turnsoft, Inc. devices

FDA 510(k) Submission Details - K923173

510(k) Number K923173 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 30, 1992
Decision Date November 06, 1992
Days to Decision 129 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
At panel average
Panel avg: 129d · This submission: 129d
Pathway characteristics
Predicate-based equivalence.

FMW Device Classification - Class 1, General Controls

Product Code FMW Cover, Mattress (medical Purposes)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6190
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FMW Cover, Mattress (medical Purposes)

All 7
Devices cleared under the same product code (FMW) and FDA review panel - the closest regulatory comparables to K923173.
Z-NET
K001003 · Demite Limited · Dec 2001
EVENT ALLERGEN BARRIERS, EVENT MATTRESS ENCASING, EVENT DUVET ENCASING, EVENT PILLOW ENCASING, EVENT BEDDING SYSTEM
K992702 · Allergy Direct · Nov 1999
INTERVENT ALLERGEN EXCLUSION TECHNOLOGY, INTERVENT BEDDING SYSTEM, INTERVENT MATTRESS INTERLINER, INTERVIEW PILLOW
K940327 · W.L. Gore & Associates, Inc. · Feb 1994
DISPOSABLE STERILE TABLE TOP COVER FOR HYDRADJUST
K902446 · Mallinckrodt Group, Inc. · Aug 1990
MATTRESS COVER, ANTI-MICROBIAL
K832483 · American Threshold Industries, Inc. · Feb 1984